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Article ? AI-assigned paper type based on the abstract. Classification may not be perfect — flag errors using the feedback button. Tier 2 ? Original research — experimental, observational, or case-control study. Direct primary evidence. Human Health Effects Policy & Risk Sign in to save

Internalization and cytotoxicity of polystyrene microplastics in human umbilical vein endothelial cells

Journal of Applied Toxicology 2022 42 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 55 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Yan-Yang Lu, Yan-Yang Lu, Yan-Yang Lu, Yan-Yang Lu, Yan-Yang Lu, Yan-Yang Lu, Yan-Yang Lu, Yan-Yang Lu, Yan-Yang Lu, Yan-Yang Lu, Meiping Tian, Yan-Yang Lu, Yan-Yang Lu, Yan-Yang Lu, Yan-Yang Lu, Meiyi Cao, Meiyi Cao, Meiyi Cao, Meiping Tian, Meiyi Cao, Meiping Tian, Qingyu Huang Qingyu Huang Meiping Tian, Qingyu Huang Qingyu Huang Meiping Tian, Qingyu Huang Meiping Tian, Qingyu Huang Qingyu Huang Qingyu Huang

Summary

Researchers investigated the uptake and toxicity of 1-micrometer polystyrene microplastics in human umbilical vein endothelial cells. The study found that interaction between the cells and microplastics was very low, with less than 4% of cells taking up particles even at high concentrations, and no significant inflammation, autophagy, or oxidative stress responses were observed at tested exposure levels.

Polymers
Study Type In vitro

Ubiquitous micro(nano)plastics (MNPs) are emerging environmental pollutants, which pose a potential threat to human health. When MNPs enter the blood circulatory system, vascular endothelium is one of the most important target organs that directly interact with the MNPs. However, little is known about the cytotoxicity of MNPs to vascular endothelial cells. In this study, we investigated the uptake and cytotoxic effects of polystyrene MNPs with a particle size of 1 μm (1-μm PS-MNPs) on human umbilical vein endothelial cells (HUVECs) in vitro. Our study found that interaction between HUVECs and 1-μm PS-MNPs was at a very low level. Even at the high exposure concentration of 25 μg/mL, the percentage of HUVECs combined with fluorescent 1-μm PS-MNPs was only 3.80% using flow cytometry analysis. Moreover, there were no significant differences in inflammation, autophagy, reactive oxygen species (ROS) level, lactate dehydrogenase (LDH) release, and adhesion molecule expression following exposure to 1-μm PS-MNPs (5, 10, and 25 μg/mL) for 48 h, except for a remarkable decrease in cell viability at the extremely high concentration of 100 μg/mL. Herein, 1-μm PS-MNPs showed a low level of acute toxicity to HUVECs in vitro, and we expect these results contribute to the further risk assessment of MNPs on human health.

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